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3-Hydroxy-2-nitropyridine

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3-Hydroxy-2-nitropyridine Basic information

Product Name:
3-Hydroxy-2-nitropyridine
Synonyms:
  • 2-nitro-3-pyridino
  • 2-Nitro-pyridin-3-ol
  • 3-HYDROXY-2-NITROPYRIDINE
  • 3-PYRIDINOL, 2-NITRO-
  • 2-NITRO-3-PYRIDINOL
  • 3-Hydroxy-2-Nitro Pyridine 2-Nitro-3-Hydroxy Pyridine
  • 3-HYDROXY-2-NITROPYRIDINE 97%
  • TIMTEC-BB SBB004168
CAS:
15128-82-2
MF:
C5H4N2O3
MW:
140.1
EINECS:
239-191-2
Product Categories:
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Pyridine
  • NITRO
  • blocks
  • Pyridines derivates
  • CHIRAL CHEMICALS
  • NitroCompounds
  • Pyridines
  • Heterocycles
  • 15128-82-2
Mol File:
15128-82-2.mol
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3-Hydroxy-2-nitropyridine Chemical Properties

Melting point:
69-71 °C (lit.)
Boiling point:
256.56°C (rough estimate)
Density 
1.5657 (rough estimate)
refractive index 
1.4800 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly, Heated)
form 
Crystalline Powder
pka
0.31±0.22(Predicted)
color 
Yellow
BRN 
124473
InChIKey
QBPDSKPWYWIHGA-UHFFFAOYSA-N
CAS DataBase Reference
15128-82-2(CAS DataBase Reference)
EPA Substance Registry System
3-Hydroxy-2-nitropyridine (15128-82-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-36
WGK Germany 
3
RTECS 
UU7715000
Hazard Note 
Irritant
HS Code 
29333990
Toxicity
mouse,LD50,intravenous,180mg/kg (180mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#04089,

MSDS

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3-Hydroxy-2-nitropyridine Usage And Synthesis

Chemical Properties

yellow crystalline powder

Uses

3-Hydroxy-2-nitropyridine may be used in the synthesis of novel sulfonates that are potent inhibitors of cell proliferation and tubulin polymerization.

Preparation

Synthesis of 3-hydroxy-2-nitropyridine: add 10g of 3-hydroxypyridine, 80ml of ethyl acetate, 4.2g of KNO3 and 21ml of acetic anhydride into a 250mL three-necked flask, and heat at 45°C with magnetic stirring After the reaction is completed, it is cooled to room temperature, filtered with suction, washed with a small amount of ethyl acetate for 1 to 2 times, the filtrate is taken to adjust the pH to neutrality with saturated NaOH solution, and extracted with ethyl acetate for 3 to 4 times. , take the extract and add activated carbon and heat under reflux for 1 hour, cool and filter, take the filtrate, dry with anhydrous magnesium sulfate, filter, concentrate on a rotary evaporator, and dry in a drying oven. 11.9 g of 3-hydroxy-2-nitropyridine was obtained with a yield of 81%.

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